[Asia Economy Reporter Minwoo Lee] IGEN announced on the 14th that it observed safety and efficacy after completing Phase 1 clinical trials of the shingles prevention vaccine 'EG-HZ' in Australia.


The trial involved a total of 40 healthy adults divided into five groups: one group receiving the active comparator GlaxoSmithKline (GSK)'s 'Shingrix' alone, and four groups receiving different formulations of 'EG-HZ'. After double-blinding both researchers and subjects, 'EG-HZ' and Shingrix were administered intramuscularly twice at two-month intervals. Observations were made at 60 days after the first vaccination, 90 days (30 days after the second vaccination), and 240 days, comparing the control group (Shingrix alone) with the test groups.



IGEN stated, "Through this clinical trial, we confirmed efficacy comparable to GSK's Shingrix as well as the safety and tolerability of EG-HZ." They added, "We plan to initiate licensing negotiations with overseas companies starting in the second half of this year and also intend to apply for Phase 2 clinical trials domestically."


This content was produced with the assistance of AI translation services.

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